Echinacoside Alleviates Carbon Tetrachloride‐Induced Chronic Liver Injury by Modulating the <scp>NF</scp>‐<scp>κB</scp>/<scp>NLRP3</scp> Inflammasome Pathway

The purpose of this study was to investigate the protective effect of echinacoside (Ech) on carbon tetrachloride (CCL4)-induced chronic liver injury in rats and its potential mechanisms. Thirty Sprague-Dawley (SD) rats were randomly divided into five groups: the Control group, the CCL4 group, the CCL4 + Ech 25 mg/kg group, the CCL4 + Ech 50 mg/kg group, and the CCL4 + Ech 100 mg/kg group. The rats were injected intraperitoneally with CCL4 solution twice a week to induce chronic liver injury, and Ech intervention lasted for 4 weeks. After the intervention, the liver and blood samples from rats were collected for subsequent analysis. Ech effectively reduced the levels of serum liver injury markers (alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, alkaline phosphatase, and total bilirubin), attenuated the hepatocyte degeneration and necrosis, improved the severity of liver fibrosis, and inhibited the local inflammatory response of the liver in a dose-dependent manner. Ech effectively mitigated CCL4-induced chronic liver injury in rats by downregulating the NF-κB/NLRP3 inflammasome pathway.

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Publication Details

Journal
Chemical Biology & Drug Design
Published
2024-09-01
DOI
https://doi.org/10.1111/cbdd.14616
Citations
3
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
1.40
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article

Echinacoside Alleviates Carbon Tetrachloride‐Induced Chronic Liver Injury by Modulating the NF‐κB/NLRP3 Inflammasome Pathway

Juan Liu, Ye‐jun Yang
3 citations
Chemical Biology & Drug Design
Drug-Induced Hepatotoxicity and Protection
1.40
article

Echinacoside Alleviates Carbon Tetrachloride‐Induced Chronic Liver Injury by Modulating the NF‐κB/NLRP3 Inflammasome Pathway

Juan Liu, Ye‐jun Yang
article en
3 citations

Abstract

The purpose of this study was to investigate the protective effect of echinacoside (Ech) on carbon tetrachloride (CCL4)-induced chronic liver injury in rats and its potential mechanisms. Thirty Sprague-Dawley (SD) rats were randomly divided into five groups: the Control group, the CCL4 group, the CCL4 + Ech 25 mg/kg group, the CCL4 + Ech 50 mg/kg group, and the CCL4 + Ech 100 mg/kg group. The rats were injected intraperitoneally with CCL4 solution twice a week to induce chronic liver injury, and Ech intervention lasted for 4 weeks. After the intervention, the liver and blood samples from rats were collected for subsequent analysis. Ech effectively reduced the levels of serum liver injury markers (alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, alkaline phosphatase, and total bilirubin), attenuated the hepatocyte degeneration and necrosis, improved the severity of liver fibrosis, and inhibited the local inflammatory response of the liver in a dose-dependent manner. Ech effectively mitigated CCL4-induced chronic liver injury in rats by downregulating the NF-κB/NLRP3 inflammasome pathway.

Chemical Biology & Drug DesignVol. 104(3)
Changzhou Third People's Hospital (CN)
Openalex Percentile: Top 19%
Drug-Induced Hepatotoxicity and Protection
1.40
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